Identification of PRMT5 as a therapeutic target in cholangiocarcinoma
type: CreativeWork
description: Cholangiocarcinoma (CCA) remains a highly aggressive malignancy characterized by poor prognosis and limited response to standard therapies, despite recent advances in drug discovery. This highlights the urgent need for novel and more effective treatment strategies. In the context of precision medicine and molecularly targeted therapies, understanding the genetic and epigenetic mechanisms underlying CCA development and progression is crucial. This study aims to explore the role of Protein Arginine Methyltransferase 5 (PRMT5) in cholangiocarcinoma, focusing on its functional implications, molecular interactions, and potential as a therapeutic target. Experimental in vitro models were established to evaluate the effects of PRMT5 inhibition on CCA cell proliferation and viability using specific PRMT5 inhibitors. Given that PRMT5 forms a hetero-octameric complex with Methylosome Protein 50 (MEP50), the study also investigated MEP50 expression and its functional relationship with PRMT5. Preliminary evidence suggests that both PRMT5 and MEP50 are overexpressed in cholangiocarcinoma and may play a crucial role in tumor growth and progression. These findings contribute to the understanding of PRMT5-mediated oncogenic mechanisms and support the potential of PRMT5 as a novel therapeutic target in CCA.
abstract: Cholangiocarcinoma (CCA) remains a highly aggressive malignancy characterized by poor prognosis and limited response to standard therapies, despite recent advances in drug discovery. This highlights the urgent need for novel and more effective treatment strategies. In the context of precision medicine and molecularly targeted therapies, understanding the genetic and epigenetic mechanisms underlying CCA development and progression is crucial. This study aims to explore the role of Protein Arginine Methyltransferase 5 (PRMT5) in cholangiocarcinoma, focusing on its functional implications, molecular interactions, and potential as a therapeutic target. Experimental in vitro models were established to evaluate the effects of PRMT5 inhibition on CCA cell proliferation and viability using specific PRMT5 inhibitors. Given that PRMT5 forms a hetero-octameric complex with Methylosome Protein 50 (MEP50), the study also investigated MEP50 expression and its functional relationship with PRMT5. Preliminary evidence suggests that both PRMT5 and MEP50 are overexpressed in cholangiocarcinoma and may play a crucial role in tumor growth and progression. These findings contribute to the understanding of PRMT5-mediated oncogenic mechanisms and support the potential of PRMT5 as a novel therapeutic target in CCA.
author: MARIANI, STEFANO
language: eng
keywords: Settore MED/06 - Oncologia Medica
date published: 2026-02-26T00:00:00+01:00
date modified: 2026-07-24T01:29:55Z
provider: Università di Cagliari
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: Università degli Studi di Cagliari

PropertyValue
property ID: Handle
value: https://hdl.handle.net/11584/477665